Comparison of Positive End Expiratory Pressure Titration Methods in ARDS Patients

NCT ID: NCT03281473

Last Updated: 2019-03-21

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-10-02

Study Completion Date

2019-12-31

Brief Summary

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This study aims at assessing the short-term physiological effects of 2 positive end expiratory pressure titration strategies in patients with ARDS.

Detailed Description

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Conditions

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Acute Respiratory Distress Syndrome

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Arms A

Strategy 1 - Washout period - Strategy 2

Group Type EXPERIMENTAL

Strategy 1

Intervention Type OTHER

PEEP titration according to transpulmonary-end-expiratory pressure

Strategy 2

Intervention Type OTHER

PEEP titration according to chest wall elastance measurement

Arms B

Strategy 2 - Washout period - Strategy 1

Group Type EXPERIMENTAL

Strategy 1

Intervention Type OTHER

PEEP titration according to transpulmonary-end-expiratory pressure

Strategy 2

Intervention Type OTHER

PEEP titration according to chest wall elastance measurement

Interventions

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Strategy 1

PEEP titration according to transpulmonary-end-expiratory pressure

Intervention Type OTHER

Strategy 2

PEEP titration according to chest wall elastance measurement

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Age\> 18 years
* Moderate or severe ARDS
* Consent to participation obtained from a relative

Exclusion Criteria

* Protect adult
* Pregnant or breastfeeding woman
* No-affiliation to the social security scheme
* Contra-indication to the placement of an esophageal pressure measuring catheter
* Pneumothorax
* Hemodynamic and / or respiratory instability
* Extra-corporeal membrane oxygenation
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Angers

OTHER_GOV

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Study Official is required by the WHO and BELONCLE, Ass.Pr

Role: PRINCIPAL_INVESTIGATOR

Angers teatching hospital

Locations

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University Hospital

Angers, , France

Site Status RECRUITING

Countries

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France

Central Contacts

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Study Official is required by the WHO and BELONCLE, Ass.Pr

Role: CONTACT

0241353845

Facility Contacts

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François BELONCLE, Ass.Pr

Role: primary

0241353845

References

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Chean D, Courtais A, Pavlovsky B, Yvin E, Desprez C, Taillantou-Candau M, Piquilloud L, Richard JC, Mercat A, Beloncle FM. Comparison of two transpulmonary pressure-based positive end-expiratory pressure titration strategies in acute respiratory distress syndrome: a randomized crossover study. Crit Care. 2025 Sep 29;29(1):409. doi: 10.1186/s13054-025-05626-x.

Reference Type DERIVED
PMID: 41024114 (View on PubMed)

Other Identifiers

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49RC17_0220

Identifier Type: -

Identifier Source: org_study_id

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